Summary of Study ST003210

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002001. The data can be accessed directly via it's Project DOI: 10.21228/M8ZJ84 This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003210
Study TitleUntargeted metabolomics analysis on single cells and cell clusters of TNBC cell lines using mass spectrometry
Study SummaryTriple-negative breast cancer (TNBC) is more aggressive than other subtypes of breast cancer, and 40% of TNBC patients undergo recurrence and metastasis after treatments. In the metastasis process, clustered cancer cells (cell clusters) exhibited a higher ability of invasion and metastasis. On the other hand, metabolic reprogramming is closely related to the process of cancer metastasis. To explore the metabolic heterogeneity between single cells and cell clusters, mass spectrometry-based untargeted metabolomic analysis was performed on single cells and cell clusters constructed from two TNBC cell lines (MDA-MB-231 and MDA-MB-453). As a result, metabolic profiling between single cells and cell clusters were explored and metabolites contributing to cell clustering were identified.
Institute
Nanjing Medical University
Last NameWang
First NameZhongcheng
Address101Longmian Avenue, Jiangning District, Nanjing 211166, P.R. China
Email1845775254@qq.com
Phone025-86868326
Submit Date2024-04-28
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2024-05-23
Release Version1
Zhongcheng Wang Zhongcheng Wang
https://dx.doi.org/10.21228/M8ZJ84
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002001
Project DOI:doi: 10.21228/M8ZJ84
Project Title:Untargeted metabolomics analysis on single cells and cell clusters of TNBC cell lines using mass spectrometry
Project Summary:Single cells and cell clusters construcetd from two triple-negative breast cancer cell lines (MDA-MB-231 and MDA-MB-453) were used to screen differential metabolites.
Institute:NanJing Medical University
Department:School of Pharmacy
Last Name:Wang
First Name:Zhongcheng
Address:101Longmian Avenue, Jiangning District, Nanjing 211166, P.R. China
Email:1845775254@qq.com
Phone:025-86868326

Subject:

Subject ID:SU003329
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606
Species Group:Mammals

Factors:

Subject type: Cultured cells; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Sample type
SA351494UM009Breast Cancer Cell Line Blank
SA351495UM010Breast Cancer Cell Line Blank
SA351496UM001Breast Cancer Cell Line Blank
SA351497UM008Breast Cancer Cell Line Blank
SA351498UM012Breast Cancer Cell Line Blank
SA351499UM011Breast Cancer Cell Line Blank
SA351500UM002Breast Cancer Cell Line Blank
SA351501UM007Breast Cancer Cell Line Blank
SA351502UM003Breast Cancer Cell Line Blank
SA351503UM004Breast Cancer Cell Line Blank
SA351504UM006Breast Cancer Cell Line Blank
SA351505UM005Breast Cancer Cell Line Blank
SA351506UM040Breast Cancer Cell Line Cell_cluster
SA351507UM041Breast Cancer Cell Line Cell_cluster
SA351508UM042Breast Cancer Cell Line Cell_cluster
SA351509UM039Breast Cancer Cell Line Cell_cluster
SA351510UM035Breast Cancer Cell Line Cell_cluster
SA351511UM043Breast Cancer Cell Line Cell_cluster
SA351512UM036Breast Cancer Cell Line Cell_cluster
SA351513UM037Breast Cancer Cell Line Cell_cluster
SA351514UM038Breast Cancer Cell Line Cell_cluster
SA351515UM051Breast Cancer Cell Line Cell_cluster
SA351516UM050Breast Cancer Cell Line Cell_cluster
SA351517UM034Breast Cancer Cell Line Cell_cluster
SA351518UM052Breast Cancer Cell Line Cell_cluster
SA351519UM049Breast Cancer Cell Line Cell_cluster
SA351520UM048Breast Cancer Cell Line Cell_cluster
SA351521UM045Breast Cancer Cell Line Cell_cluster
SA351522UM046Breast Cancer Cell Line Cell_cluster
SA351523UM047Breast Cancer Cell Line Cell_cluster
SA351524UM044Breast Cancer Cell Line Cell_cluster
SA351525UM031Breast Cancer Cell Line Cell_cluster
SA351526UM018Breast Cancer Cell Line Cell_cluster
SA351527UM033Breast Cancer Cell Line Cell_cluster
SA351528UM020Breast Cancer Cell Line Cell_cluster
SA351529UM021Breast Cancer Cell Line Cell_cluster
SA351530UM017Breast Cancer Cell Line Cell_cluster
SA351531UM016Breast Cancer Cell Line Cell_cluster
SA351532UM013Breast Cancer Cell Line Cell_cluster
SA351533UM014Breast Cancer Cell Line Cell_cluster
SA351534UM015Breast Cancer Cell Line Cell_cluster
SA351535UM022Breast Cancer Cell Line Cell_cluster
SA351536UM019Breast Cancer Cell Line Cell_cluster
SA351537UM030Breast Cancer Cell Line Cell_cluster
SA351538UM023Breast Cancer Cell Line Cell_cluster
SA351539UM032Breast Cancer Cell Line Cell_cluster
SA351540UM028Breast Cancer Cell Line Cell_cluster
SA351541UM029Breast Cancer Cell Line Cell_cluster
SA351542UM024Breast Cancer Cell Line Cell_cluster
SA351543UM027Breast Cancer Cell Line Cell_cluster
SA351544UM025Breast Cancer Cell Line Cell_cluster
SA351545UM026Breast Cancer Cell Line Cell_cluster
SA351546UM068Breast Cancer Cell Line QCs
SA351547UM067Breast Cancer Cell Line QCs
SA351548UM066Breast Cancer Cell Line QCs
SA351549UM065Breast Cancer Cell Line QCs
SA351550UM064Breast Cancer Cell Line QCs
SA351551UM072Breast Cancer Cell Line QCs
SA351552UM071Breast Cancer Cell Line QCs
SA351553UM070Breast Cancer Cell Line QCs
SA351554UM069Breast Cancer Cell Line QCs
SA351555UM057Breast Cancer Cell Line QCs
SA351556UM056Breast Cancer Cell Line QCs
SA351557UM055Breast Cancer Cell Line QCs
SA351558UM054Breast Cancer Cell Line QCs
SA351559UM063Breast Cancer Cell Line QCs
SA351560UM058Breast Cancer Cell Line QCs
SA351561UM053Breast Cancer Cell Line QCs
SA351562UM062Breast Cancer Cell Line QCs
SA351563UM059Breast Cancer Cell Line QCs
SA351564UM061Breast Cancer Cell Line QCs
SA351565UM060Breast Cancer Cell Line QCs
SA351566UM099Breast Cancer Cell Line Single_cell
SA351567UM102Breast Cancer Cell Line Single_cell
SA351568UM101Breast Cancer Cell Line Single_cell
SA351569UM100Breast Cancer Cell Line Single_cell
SA351570UM097Breast Cancer Cell Line Single_cell
SA351571UM103Breast Cancer Cell Line Single_cell
SA351572UM095Breast Cancer Cell Line Single_cell
SA351573UM096Breast Cancer Cell Line Single_cell
SA351574UM098Breast Cancer Cell Line Single_cell
SA351575UM108Breast Cancer Cell Line Single_cell
SA351576UM110Breast Cancer Cell Line Single_cell
SA351577UM111Breast Cancer Cell Line Single_cell
SA351578UM112Breast Cancer Cell Line Single_cell
SA351579UM109Breast Cancer Cell Line Single_cell
SA351580UM094Breast Cancer Cell Line Single_cell
SA351581UM105Breast Cancer Cell Line Single_cell
SA351582UM106Breast Cancer Cell Line Single_cell
SA351583UM107Breast Cancer Cell Line Single_cell
SA351584UM104Breast Cancer Cell Line Single_cell
SA351585UM088Breast Cancer Cell Line Single_cell
SA351586UM078Breast Cancer Cell Line Single_cell
SA351587UM079Breast Cancer Cell Line Single_cell
SA351588UM080Breast Cancer Cell Line Single_cell
SA351589UM081Breast Cancer Cell Line Single_cell
SA351590UM077Breast Cancer Cell Line Single_cell
SA351591UM076Breast Cancer Cell Line Single_cell
SA351592UM073Breast Cancer Cell Line Single_cell
SA351593UM074Breast Cancer Cell Line Single_cell
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Collection:

Collection ID:CO003322
Collection Summary:Two hours before metabolite extraction, the cell culture medium was replaced with fresh medium. Single cell and cell cluster states were collected and centrifuged at 800 × g for 3 min to remove culture media. Then, the cells were resuspended in 1 mL of precooled PBS (4°C) and transferred into a 1.5 mL eppendorf tube. After removing supernatant by centrifugation at 800 × g for 3 min, the tube containing cell pellet was immediately incubated in liquid nitrogen for 1 min to quench enzyme activity and stop the degradation of metabolites.
Collection Protocol Filename:WZC_Collection_protocol.pdf
Sample Type:Cultured cells

Treatment:

Treatment ID:TR003338
Treatment Summary:MDA-MB-231 cells and MDA-MB-453 were maintained in L-15 medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin at 37 °C in a free gas exchange with atmospheric air.

Sample Preparation:

Sampleprep ID:SP003336
Sampleprep Summary:300 μL of H2O was then added to the tube, and the cells were fully lysed by an ultrasonic cell disruptor for 10 min at 4°C. After mixing, 20 μL of suspension was collected for protein quantification and subsequent data normalization. Then, methanol (precooled to −80°C) was added into the tube to make 80% methanol solution (v/v). The tube was vortexed vigorously for 5 min and centrifuged at 14,000 × g for 10 min at 4°C to remove the cell debris. Afterward, the metabolite-containing supernatant was transferred to a new tube on ice. The supernatant was evaporated to dryness in a vacuum concentrator and reconstituted in 100 μL of methanol: H2O (1:1, v/v), which was centrifuged again at 14000 × g for 15 min at 4°C to remove insoluble debris.
Sampleprep Protocol Filename:Sampleprep_protocol.pdf

Combined analysis:

Analysis ID AN005262 AN005263 AN005264 AN005265
Analysis type MS MS MS MS
Chromatography type HILIC HILIC Reversed phase Reversed phase
Chromatography system Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000
Column Agilent InfinityLab Poroshell 120 HILIC-Z (100 x 2.1mm, 2.7um) Agilent InfinityLab Poroshell 120 HILIC-Z (100 x 2.1mm, 2.7um) Phenomenex Kinetex C18 (100 x 2.1mm,2.6um) Phenomenex Kinetex C18 (100 x 2.1mm,2.6um)
MS Type ESI ESI ESI ESI
MS instrument type Orbitrap Orbitrap Orbitrap Orbitrap
MS instrument name Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap Thermo Q Exactive HF hybrid Orbitrap
Ion Mode POSITIVE NEGATIVE POSITIVE NEGATIVE
Units Peak area Peak area Peak area Peak area

Chromatography:

Chromatography ID:CH003983
Methods Filename:Chromatography_methods.pdf
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Agilent InfinityLab Poroshell 120 HILIC-Z (100 x 2.1mm, 2.7um)
Column Temperature:40
Flow Gradient:85% B (0 min) to 85% B (1 min) to 65% B (12 min) to 40% B (12.1 min) to 40% B (15 min) to 85% B (15.1 min) to 85% B (20 min), the flow gradient increases linearly between the time points mentioned.
Flow Rate:0.3 mL/min
Solvent A:100% Water; 25 mM Ammonium acetate; 25 mM Ammonium hydroxide
Solvent B:100% Acetonitrile
Chromatography Type:HILIC
  
Chromatography ID:CH003984
Methods Filename:Chromatography_methods.pdf
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Phenomenex Kinetex C18 (100 x 2.1mm,2.6um)
Column Temperature:40
Flow Gradient:10% B (0 min) to 30% B (1 min) to 95% B (19 min) to 95% B (20 min) to 10% B (20.1 min) to 10% B (23 min), the flow gradient increases linearly between the time points mentioned.
Flow Rate:0.4 mL/min
Solvent A:100% Water; 0.1% Formic acid
Solvent B:100% Acetonitrile; 0.1% Formic acid
Chromatography Type:Reversed phase

MS:

MS ID:MS004993
Analysis ID:AN005262
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:All operations and acquisitions were controlled by Xcalibur 2.0.7 (Thermo Fisher Scientific, Bremen, Germany).UPLC-HRMS data were analyzed using MS-DIAL software after conversion to mzML file format using MSConvert (Version 3.0, ProteiWizard).
Ion Mode:POSITIVE
Analysis Protocol File:MS_analysis_protocol.pdf
  
MS ID:MS004994
Analysis ID:AN005263
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:All operations and acquisitions were controlled by Xcalibur 2.0.7 (Thermo Fisher Scientific, Bremen, Germany).UPLC-HRMS data were analyzed using MS-DIAL software after conversion to mzML file format using MSConvert (Version 3.0, ProteiWizard).
Ion Mode:NEGATIVE
Analysis Protocol File:MS_analysis_protocol.pdf
  
MS ID:MS004995
Analysis ID:AN005264
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:All operations and acquisitions were controlled by Xcalibur 2.0.7 (Thermo Fisher Scientific, Bremen, Germany).UPLC-HRMS data were analyzed using MS-DIAL software after conversion to mzML file format using MSConvert (Version 3.0, ProteiWizard).
Ion Mode:POSITIVE
Analysis Protocol File:MS_analysis_protocol.pdf
  
MS ID:MS004996
Analysis ID:AN005265
Instrument Name:Thermo Q Exactive HF hybrid Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:All operations and acquisitions were controlled by Xcalibur 2.0.7 (Thermo Fisher Scientific, Bremen, Germany).UPLC-HRMS data were analyzed using MS-DIAL software after conversion to mzML file format using MSConvert (Version 3.0, ProteiWizard).
Ion Mode:NEGATIVE
Analysis Protocol File:MS_analysis_protocol.pdf
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